Disease #05861 (NEDSWMA;CPSQ1 (neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1)), OMIM:619026)
| Official abbreviation |
NEDSWMA;CPSQ1 |
| Name |
neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (CPSQ1) |
| OMIM ID |
619026 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
HPDL |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-10-23 08:54:34 +02:00 (CEST) |
| Date last edited |
2023-12-06 12:38:41 +01:00 (CET) |
Individuals
|